Methods and strains for producing bioproducts in Aureobasidium pullulans

ABSTRACT

The present disclosure provides methods for producing bioproducts from novel genetically altered strains of  Aureobasidium pullulans . Methods and materials for the construction of these strains, examination of the bioproducts and analysis and isolation of the bioproducts from genetically altered strains is provided. Genetically altered  A. pullulans  strains in which one or more genes encoding biosynthetic enzymes are knocked out is detailed and the benefits of using such strains described.

CROSS-REFERENCE

The present application is a divisional of application Ser. No. 15/212,471, filed on Jul. 18, 2016 and also claims priority to U.S. Provisional Patent Application Ser. No. 62/193,875 filed Jul. 17, 2015, the content of which is expressly incorporated herein by reference.

BACKGROUND OF THE INVENTION Field of Invention

This invention relates to genetically modified strains of Aureobasidium pullulans that are capable of producing desirable bioproducts. By altering the biochemistry of the disclosed strains via genetic manipulation, strains have been produced that no longer produce bio-contaminants such as melanin and melanin-related pigments. The presence of such pigments adds significant cost to the production of bioproducts because they must be removed prior to further processing of the desired products. Additionally, some strains described herein are modified to delete the genes encoding for biosynthetic enzymes that produce undesired products. Therefore, modified strains lacking the capacity of forming less-desired bioproducts have been constructed that form target bioproducts preferentially on cheaper substrates. Utilizing these methods and strains, production of desired products can be achieved under more economically feasible conditions, resulting in a benefit to food, pharmaceutical, industrial, biofuel and other important industries.

Background

Aureobasidium pullulans is a yeast-like fungus, perhaps best well-known as the source of the exopolysaccharide pullulan, which is commercially-produced for numerous consumer and industrial applications, such as emulsifiers, thickeners, and edible films (Leathers, Polysaccharides from eukaryotes. In: Vandamme, E. J., De Baets, S., and Steinbuchel, A., Editors. Biopolymers. Weinheim, Germany: Wiley-VCH. p. 1-35 (2002); Singh et al., Carb. Polymers, 73(4):515-31, (2008)). A. pullulans also produces other useful bioproducts, including industrial enzymes (Leathers et al., Biotech Lett., 35(10):1701-6 (2013); Rich et al., Enz. Microb. Tech., 53(1):33-37 (2013); Liu, et al., Anton Leeuw Int. J. G., 94(2):245-55 (2008); Leathers, J. Indus. Microbiol. 4(5):341-7 (1989); Kudanga et al., J. Basic Microbiol. 47(2): 138-47 (2007)), the biopolyester poly(β-L-malic acid) (Leathers and Manitchotpisit, Biotech. Lett., 35(1):83-9 (2013), and numerous bioactive compounds (Wang, et al., Bioresource Tech., 100(9):2639-41 (2009); Chi, et al., Appl. Microbiol. Biotech., 82(5):793-804 (2009); Slightom, et al., Gene, 431(1-2):67-79 (2009)), including an extracellular dense “oil” that accumulates on the bottom of the fermentation flask (Nagata, et al., in Biosci. Biotech. Biochem., 57(4):638-42 (1993)). A partial structure of this oil suggested that they were 3,5-dihydroxydecanoyl and 5-hydroxy-2-decanoyl esters of arabitol and mannitol (Kurosawa, et al., Biosci., Biotech. Biochem., 58(11):2057-60 (1994)) and that these polyol lipids exert an anti-proliferative effect on cancer cell lines (Isoda and Nakahara, J. Ferment. Bioeng., 84(5):403-406 (1997)).

Different strains of A. pullulans demonstrate different phenotypes with regards to bioproducts produced and can be genetically distinguished from each other. (Manitchotpisit, et al., Mycol. Res., 133(10):1107-20 (1997)). It has been noted that about half of all strains of this filamentous fungus produced oils, with certain genetically-related strains showing the highest yields (Id.; Manitchotpisit, et al., Biotech. Lett., 33(6):1151-57 (2011); Manitchotpisit, et al., World J. Micro. Biotech., 30(8):2199-2204 (2014)). Oil colors range from bright yellow to malachite and more than half of the strains produced oil that was fluorescent. Preliminary studies suggest that these pigments are likely a result of contamination by melanin, melanin breakdown products, and melanin intermediates, which are common pigments associated with A. pullulans. The oils have demonstrated biosurfactant properties (Manitchotpisit, et al. (2011)). Additionally, it has been shown that oil from different strains differentially inhibits mammalian cancer cell lines (Manitchotpisit, et al. (2014)). Recently, these microbial oils have been demonstrated to exhibit potent selective antibacterial activities against certain Streptococcal species (Bischoff, et al., J. Antibiot., (2015) 68:642-45).

The antibacterial activities of these microbial oils (also termed “liamocins”) may have potential applications, similar to other glycolipids or A. pullulans secreted metabolites, as a veterinary treatment (Cortes-Sanchez, et al., Microbiol. Res., 168(1):22-32 (2013)), an antifouling agent (Gao, et al., Marine Poll. Bull., 77(1-2):172-6 (2013); Abdel-Lateff, et al., Nat. Prod. Commns., 4(3):389-94 (2009)), and a phytopathogen control agent (Le Dang, et al., J. Agr. Food Chem., 62(15):3363-70 (2014)). In addition, the medium-chain dihydroxydecanoate fatty acid is promising as a potential chemical feedstock for the synthesis of a wide variety of commercially relevant products, such as biosurfactants and polymers (Tang, et al., Polymer Chem., 5(9):3231-37 (2014); Schneiderman, et al., J. Chem. Edu., 91(1); 131-5 (2014).

A. pullulans is also used for production the antibiotic aureobasidin and β-glucan. Production of both of these products could be improved by utilizing strains that are no longer producing melanin or melanin-related pigments. In addition, A. pullulans was recently shown to produce significant amounts of intracellular lipids (Wang et al., Process Biochem., 49(5):725-31 (2014)), which may have potential for biodiesel or specialty oil production (Sitepu et al., Biotech. Adv., 32(7):1336-1360 (2014)).

As alluded to above, one of the problems with using A. pullulans for bioproduct formation is that most strains produce dark melanin-associated pigments that contaminate the final desired product. These contaminating pigments can be removed by treatment with activated charcoal or hydrogen peroxide, but further purification with ultrafiltration and ion exchange resins are typically required. These clean up steps frequently result in loss of the desired bioproduct and add further cost to the manufacturing process (Mishra and Vuppu, Res. J. Microbiol. Biotech., 2:16-19 (2013); Leathers, Appl. Microbiol. Biotech., 62(5-6):468-473 (2003)). Oils and other bioproducts free of melanin or melanin-related pigments would be easier and cheaper to purify, making them more valuable and more economically feasible to produce. Thus, downstream products, such as biodiesel and food additives and preservatives would also be cheaper to produce.

Therefore, it is an object of the present invention to provide methods and strains of A. pullulans for the production of desired bioproducts as well as melanin-free bioproducts. Using the strains and methodologies presented here provides not only for a cheaper alternative to the use of non-modified strains, but also allows for a more ecologically responsible approach for the production of some bioproducts.

SUMMARY OF THE INVENTION

One aspect of the present invention is providing a biologically pure strain lacking mannitol-1-phosphate-dehydrogenase activity. In one instance, the biologically pure strain is the A. pullulans strain MpdKO.

An additional aspect of the invention disclosed herein is providing a biologically pure strain lacking mannitol-dehydrogenase activity. In one instance, the biologically pure strain is the A. pullulans strain Mdh2KO.

It is another object of the invention disclosed herein to provide a biologically pure strain lacking polyketide-synthase activity. In one instance, the biologically pure strain is the A. pullulans strain PksKO.

Further provided herein is a method of producing arabitol-liamocins, comprising the steps of: a) growing a culture of A. pullulans comprising a biologically pure strain lacking a functional MPD1 gene under conditions sufficient to support the production of arabitol-liamocins, such as growth media having a substantial absence of arabitol; and b) collecting the arabitol-liamocins from at least part of the culture, thereby producing arabitol-liamocins. In some embodiments, the biologically pure strain is the deposited strain NRRL 67079. In still other embodiments, the growth medium contains glucose as the sole carbon source.

An additional embodiment provided herein is a method of producing one or more bioproducts, comprising the steps of: growing a culture of A. pullulans comprising a biologically pure strain lacking a functional MDH2 gene and lacking a functional MPD1 gene under conditions sufficient to support the production of one or more bioproducts including liamocins and exophilins; and collecting one or more of the bioproducts from at least part of the culture, thereby producing the bioproduct. In some embodiments of this methodology, the growth of the culture occurs in or on a growth medium containing glucose or fructose as the sole carbon source. In specific embodiments, the bioproduct is an exophilin. In other embodiments, the bioproduct is a liamocin with a lactose, glucose, mannose, galactose, arabinose, xylose, glucitol, galactitol, xylitol, ribitol, threitol, erythritol, or glycerol head group. In still another embodiment, the bioproduct is a fructose-liamocin (a liamocin with a fructose head group).

Another invention detailed herein is a method of producing massoia lactone from a culture of A. pullulans, comprising the steps of: growing a culture of A. pullulans comprising a biologically pure strain lacking a functional PKS gene under conditions sufficient to support the production of massoia lactone; and b) collecting the massoia lactone from at least part of the culture, thereby producing massoia lactone. In a particular embodiment, the biologically pure strain utilized in practicing this methodology is the deposited strain NRRL 67080.

In yet another embodiment of the invention, this application discloses a method of producing a substantially melanin-free bioproduct from a culture of A. pullulans, comprising the steps of: a) growing a culture of A. pullulans comprising a biologically pure strain lacking a functional PKS4 gene under conditions sufficient to support the production of the bioproduct; and b) collecting the bioproduct from at least part of the culture, thereby producing a substantially melanin-free bioproduct. In some instances the bioproduct produced is one or more of pullulan, a liamocin, a lactone, an exophilin, poly(β-malic acid), β-glucan, aureobasidin, an intracellular fatty acid, and a triacylglycerol. In specific embodiments, the bioproduct is a liamocin, such as those with a head group comprised of lactose, glucose, mannose, galactose, arabinose, xylose, glucitol, galactitol, xylitol, ribitol, threitol, erythritol, or glycerol. In other embodiments, the bioproduct is massoia lactone. This methodology can be practiced using the biologically pure deposited strain NRRL 67080.

Also provided herein are compositions containing the novel fructose-liamocin (liamocin with a fructose head group). Such fructose-liamocins can be produced utilizing a biologically pure A. pullulans strain lacking a functional MDH2 gene and lacking a functional MPD1 gene.

INCORPORATION BY REFERENCE

All publications, patents and patent applications mentioned in this specification are herein incorporated by reference to the same extent as if each individual publication, patent or patent application was specifically and individually indicated to be incorporated by reference.

BRIEF DESCRIPTION OF THE DRAWINGS

The patent application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawing(s) will be provided by the Office upon request and payment of the necessary fee.

The novel features of the invention are set forth with particularity in the claims. Features and advantages of the present invention are referred to in the following detailed description, and the accompanying drawings of which:

FIG. 1 provides an example of liamocin structures. Man-A2 (left) contains three 0-linked 3,5-dihydroxydecanoate groups with a mannitol headgroup. Ara-A2 (right) contains an arabitol headgroup. R═OH or O-acetyl. A2 defines the R group as 0-acetyl.

FIG. 2 provides a proposed biosynthetic pathway for production of mannitol and arabitol in A. pullulans.

FIG. 3 provides a diagram of DNA constructs used for deletion of the (A) pks4 gene and (B) the mpd1 gene in A. pullulans. The A. pullulans trans elongation factor promoter (TEF Prom) was fused to the Escherichia coli hygromycin phosphotransferase gene (hph), and the TrypC terminator from Aspergillus nidulans (TrpC Term) obtained from plasmid pCSN43 (www.fgsc.net/fgn41/carroll.html). The hygromycin resistant expression cassette was then flanked with 5′ upstream and 3′ downstream regions of either the pks4 or mpd1 genes. Primers used for PCR amplification of DNA fragments are shown with arrows designating the direction of synthesis. Size of the constructs (base pairs) used in our examples is shown at the bottom.

FIG. 4 provides MALDI-TOF spectra of purified liamocins from A. pullulans NRRL 50384 (top) and A. pullulans MpdKO transformant grown on PM medium with 50 g/L glucose.

FIG. 5 provides MALDI-TOF spectra of purified liamocins from A. pullulans NRRL 50384 (top) and A. pullulans MpdKO transformant grown on PM medium with 50 g/L fructose.

FIG. 6 provides a comparison of melanin pigments between cultures of A. pullulans NRRL 50384 (left) and A. pullulans PksKO transformant (right).

FIG. 7 provides a comparison of pigments in liamocins purified from A. pullulans NRRL 50384 (left) and A. pullulans PksKO transformant (right).

FIG. 8 provides MALDI-TOF spectra of purified liamocins from A. pullulans NRRL 50384 (top) and A. pullulans PksKO transformant.

FIG. 9 provides a MALDI-TOF spectrum of purified massoia lactone from A. pullulans PksKO transformant.

FIG. 10 provides MALDI-TOF spectra of purified liamocins from A. pullulans Mdh2KO transformant (top) and A. pullulans Mdh2KO/Mpd1KO transformant grown on PM medium with 50 g/L glucose.

FIG. 11 provides MALDI-TOF spectra of purified liamocins from A. pullulans Mdh2KO transformant (top) and A. pullulans Mdh2KO/Mpd1KO transformant grown on PM medium with 50 g/L fructose.

FIG. 12 provides GC profiles (as peracetates) of purified and treated liamocins from A. pullulans Mdh2.Mpd1KO transformant grown on PM medium with 50 g/L fructose.

FIG. 13 provides a generic fructose-liamocin structure in which the fructose head group and the variable R₁ and R₂ groups are indicated.

STATEMENT OF DEPOSIT

Strains representative of the inventions disclosed herein were deposited on Aug. 6, 2015 under the terms of the Budapest Treaty with the Agricultural Research Service (ARS) Patent Culture Collection. A representative A. pullulans Mpd1KO strain (a strain with a disrupted MPD1 gene (SEQ ID NO. 1)) was deposited under ARS Patent Culture Collection Reference No. NRRL 67079 and lacks a functional MPD1 gene. A representative A. pullulans Psk4KO strain (a strain with a disrupted PSK4 gene (SEQ ID NO. 4)) was deposited under ARS Patent Culture Collection Reference No. NRRL 67080 and lacks a functional PSK4 gene. Strains representative of the inventions disclosed herein were also deposited on Jul. 12, 2016 under the terms of the Budapest Treaty with the Agricultural Research Service (ARS) Patent Culture Collection. A representative A. pullulans Mdh2KO/Mpd1KO strain (a strain with a disrupted MPD1 gene (SEQ ID NO. 1) and a disrupted MDH2 gene (SEQ ID NO. 3)) was deposited under ARS Patent Culture Collection Reference No. NRRL 67281 and lacks a functional MPD1 gene and a functional MDH2 gene. A representative A. pullulans Mdh2KO strain (a strain with a disrupted MDH2 gene (SEQ ID NO. 3) was deposited under ARS Patent Culture Collection Reference No. NRRL 67282 and lacks a functional MDH2 gene. The microorganism deposits were made under the provisions of the “Budapest Treaty on the International Recognition of the Deposit of Microorganisms for the Purposes of Patent Procedure”. All restrictions on the availability to the public of these deposited microorganisms will be irrevocably removed upon issuance of a United States patent based on this application. For the purposes of this invention, any A. pullulans strains having the identifying characteristics of NRRL 67079, NRRL 67080, NRRL 67281, or NRRL 67282, including subcultures and variants thereof which have the identifying characteristics and activity as described herein are included.

DETAILED DESCRIPTION OF THE INVENTION

Preferred embodiments of the present invention are shown and described herein. It will be obvious to those skilled in the art that such embodiments are provided by way of example only. Numerous variations, changes, and substitutions will occur to those skilled in the art without departing from the invention. Various alternatives to the embodiments of the invention described herein may be employed in practicing the invention. It is intended that the included claims define the scope of the invention and that methods and structures within the scope of these claims and their equivalents are covered thereby.

Technical and scientific terms used herein have the meanings commonly understood by one of ordinary skill in the art to which the instant invention pertains, unless otherwise defined. Reference is made herein to various materials and methodologies known to those of skill in the art. Standard reference works setting forth the general principles of recombinant DNA technology include Sambrook et al., “Molecular Cloning: A Laboratory Manual”, 2d ed., Cold Spring Harbor Laboratory Press, Plainview, N.Y., 1989; Kaufman et al., eds., “Handbook of Molecular and Cellular Methods in Biology and Medicine”, CRC Press, Boca Raton, 1995; and McPherson, ed., “Directed Mutagenesis: A Practical Approach”, IRL Press, Oxford, 1991. Standard reference literature teaching general methodologies and principles of fungal genetics useful for selected aspects of the invention include: Sherman et al. “Laboratory Course Manual Methods in Yeast Genetics”, Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y., 1986 and Guthrie et al., “Guide to Yeast Genetics and Molecular Biology”, Academic, New York, 1991.

Any suitable materials and/or methods known to those of skill can be utilized in carrying out the instant invention. Materials and/or methods for practicing the instant invention are described. Materials, reagents and the like to which reference is made in the following description and examples are obtainable from commercial sources, unless otherwise noted. This invention teaches methods and describes tools for producing genetically altered strains of A. pullulans.

As used in the specification and claims, use of the singular “a”, “an”, and “the” include plural references unless the context clearly dictates otherwise.

The term “A. pullulans” refers to Aureobasidium pullulans.

The terms isolated, purified, or biologically pure as used herein, refer to material that is substantially or essentially free from components that normally accompany the referenced material in its native state.

The term “about” is defined as plus or minus ten percent of a recited value. For example, about 1.0 g means 0.9 g to 1.1 g.

The phrases “substantially free of melanin,” “substantially melanin-free,” or other grammatical variations thereof refer to cultures, media, bioproducts, etc. which contain no detectable melanin produced by the same microorganism producing a bioproduct of interest prior to any downstream process which would remove melanin. These phrases also refer to cultures, media, bioproducts, etc. to which melanin is added from an exogenous source, but which otherwise meet the definition above.

The phrases “substantially free of arabitol,” “substantially arabitol-free,” or other grammatical variations thereof refer to cultures, media, etc., which contain no arabitol, or contain insufficient arabitol (when viewed as a sole carbon source) to support more than three doubling times of a microbe producing a desired bioproduct.

The terms MPD and MPD1 are defined as the gene encoding mannitol-1-phosphate-dehydrogenase in A. pullulans. (SEQ ID NO. 1)

The term MDH1 is defined as the gene encoding a putative mannitol dehydrogenase in A. pullulans that is likely a mitochondrial enzyme (cytochrome) mainly involved in converting mannitol to fructose. (SEQ ID NO. 2)

The term MDH2 is defined as the gene encoding mannitol-dehydrogenase in A. pullulans. (SEQ ID NO. 3)

The terms PKS and PKS4 are defined as the gene encoding polyketide synthase in A. pullulans. (SEQ ID NO. 4)

The term URA3 is defined as the gene encoding Orotidine-5′-phosphate (OMP) decarboxylase in A. pullulans. (SEQ ID NO. 5)

The terms “MpdKO”, “Mpd1KO”, “Mdh1KO”, “Mdh2KO”, “PksKO”, “Psk4KO”, and grammatical variations thereof, refer to strains of A. pullulans which lack the functional indicated gene because of targeted genetic disruption of the indicated gene. These terms can be used in combination to refer to strains with multiple disrupted genes, e.g., “Mdh2KO/Mpd1KO” refers to a strain in which both the MDH2 and MPD1 genes have been disrupted. These terms can also be used to identify the specific genetically disrupted strains described herein—for example “MpdKO” can refer to an A. pullulans strain in which the MPD1 gene has been disrupted with the cassette of SEQ ID NO. 6 and “PksKO” can refer to an A. pullulans strain in which the PKS4 gene has been disrupted with the cassette of SEQ ID NO. 7.

Some embodiments of the present invention involve creating strains which lack a functional gene. As used herein, the phrase “strains lacking a functional gene”, and grammatical variations thereof, refers to a microbial strain in which the referenced gene has been mutated, deleted, or otherwise modified such that the gene no longer produces a functional protein. Thus, the phrase includes mutational, insertional and deletional variants of the subject gene. Such variants can include alteration of transcriptional regulatory machinery, translational regulatory machinery, coding regions and non-coding regions. Non-limiting examples of such changes include insertion of point mutations, insertions or deletions causing frame shift mutations, deletions of some or all of the coding sequence, alterations rendering promoters or start codons inoperable, and alterations rendering stop codons inoperable. Additionally, introduction of genetic elements that interfere with translation, but do not directly affect the target gene itself (e.g., introduction of anti-sense RNA encoding plasmids or other genetic elements) are also included. Those skilled in the art will readily recognize methodologies capable of producing strains lacking a functional gene.

Mutational, insertional, and deletional variants of the disclosed nucleotide sequences and genes can be readily prepared by methods which are well known to those skilled in the art. It is well within the skill of a person trained in this art to make mutational, insertional, and deletional mutations which are equivalent in function to the specific ones disclosed herein.

In some embodiments, strains of A. pullulans are genetically modified to deplete the strain of the capacity to produce a particular biosynthetic enzyme. In other embodiments, strains of A. pullulans are genetically modified to deplete the strain of the capacity to produce more than one biosynthetic enzyme. In some embodiments, depleting the capacity of a strain of A. pullulans to produce one or more biosynthetic enzymes results in a biochemical alteration in the resulting strain leading to production of a desired bioproduct. In still other embodiments, depleting the capacity of a strain of A. pullulans to produce a biosynthetic enzyme prevents that strain from producing an unwanted or undesirable bio-contaminant that would otherwise be co-produced along with a desired bioproduct. The discussion below provides techniques that can be used to produce genetically modified strains of A. pullulans. The discussion is not limiting in any way on the scope of the inventions disclosed herein, and any current or future techniques which allow for the production of such strains by one of skill in the art can be utilized. Following the teachings herein and using knowledge and techniques well known in the art, the skilled worker will be able to make a large number of operative embodiments having equivalent functionality to those listed and contemplated herein.

Molecular Biological Methods

An isolated nucleic acid is a nucleic acid the structure of which is not identical to that of any naturally occurring nucleic acid. The term therefore covers, for example, (a) a DNA which has the sequence of part of a naturally occurring genomic DNA molecule but is not flanked by both of the coding or noncoding sequences that flank that part of the molecule in the genome of the organism in which it naturally occurs; (b) a nucleic acid incorporated into a vector or into the genomic DNA of a prokaryote or eukaryote in a manner such that the resulting molecule is not identical to any naturally occurring vector or genomic DNA; (c) a separate molecule such as a cDNA, a genomic fragment, a fragment produced by polymerase chain reaction (PCR), or a restriction fragment; and (d) a recombinant nucleotide sequence that is part of a hybrid gene, i.e., a gene encoding a fusion protein. Specifically excluded from this definition are nucleic acids present in mixtures of (i) DNA molecules, (ii) transformed or transfected cells, and (iii) cell clones, e.g., as these occur in a DNA library such as a cDNA or genomic DNA library.

The term recombinant nucleic acids refers to polynucleotides which are made by the combination of two otherwise separated segments of sequence accomplished by the artificial manipulation of isolated segments of polynucleotides by genetic engineering techniques or by chemical synthesis. In so doing one may join together polynucleotide segments of desired functions to generate a desired combination of functions.

Recombinant host cells, in the present context, are those which have been genetically modified to contain an isolated nucleic molecule of the instant invention. The nucleic acid can be introduced by any means known to the art which is appropriate for the particular type of cell, including without limitation, transformation, lipofection, electroporation or any other methodology known by those skilled in the art.

In practicing some embodiments of the invention disclosed herein, it is useful to modify the genomic DNA of a strain of A. pullulans or another target organism. In many embodiments, such modification involves deletion of all or a portion of a target gene, including but not limited to the open reading frame of the target gene, transcriptional regulators such as promoters of the target gene, and any other regulatory nucleic acid sequences positioned 5′ or 3′ from the open reading frame. Such deletional mutations can be achieved using any technique known to those of skill in the art. One such approach is to utilize a “deletion cassette” or “knockout cassette” (See, e.g., Fonzi and Irwin, Genetics, 134(3):717-28 (1993)). Knockout cassettes typically comprise at least three nucleic acid components: 1) an isolated nucleic acid that is homologous to a 5′ region of a target gene or other locus; 2) an isolated nucleic acid that serves as a marker; and 3) an isolated nucleic acid that his homologous to a 3′region of a target gene or other locus. Other genetic elements can be included, depending on the particular application and design of the cassette. A knockout cassette is then introduced into an organism of interest via any appropriate means known in the art (e.g., electroporation). Taking advantage of intracellular processes such as homologous recombination, the knockout cassette integrates into the genome of the target cell. In some instances, this initial integration event deletes all or part of the target gene or locus replacing the wild type genomic DNA and deleting or “knocking out” the wild type DNA between the 5′ and 3′ nucleic acids of the knockout cassette. In other instances, the initial integration of the knockout cassette is followed by a subsequent recombinatorial event that results in the deletion of the target gene or locus, such as by introducing heterologous DNA flanking the gene or locus of interest and inducing homologous recombination between the two heterologous DNA segments. Knockout cassettes can be constructed in a variety of ways known in the art (e.g., split marker transformation). Knockout cassettes can contain multiple markers that allow one skilled in the art to detect initial integration events and subsequent recombinatorial events.

Where a recombinant nucleic acid is intended for expression, cloning, or replication of a particular sequence, DNA constructs prepared for introduction into a prokaryotic or eukaryotic host will typically comprise a replication system (i.e. vector) recognized by the host, including the intended DNA fragment encoding the desired polypeptide, and can also include transcription and translational initiation regulatory sequences operably linked to the polypeptide-encoding segment. Expression systems (expression vectors) may include, for example, an origin of replication or autonomously replicating sequence (ARS) and expression control sequences, a promoter, an enhancer and necessary processing information sites, such as ribosome-binding sites, RNA splice sites, polyadenylation sites, transcriptional terminator sequences, and mRNA stabilizing sequences. Signal peptides may also be included where appropriate from secreted polypeptides of the same or related species, which allow the protein to cross and/or lodge in cell membranes or be secreted from the cell.

In some instances, a host cell other than A. pullulans can serve as a recipient for recombinant DNA. For example, a bacterial host may be utilized to clone a plasmid in which a deletion cassette is constructed, replicated, or analyzed. In such instances, a recombinant DNA fragment may require an appropriate promoter and other necessary vector sequences that can be readily selected so as to be functional in the host. Examples of workable combinations of cell lines and expression vectors are described in Sambrook et al. (1989) vide infra; Ausubel et al. (Eds.) (1995) Current Protocols in Molecular Biology, Greene Publishing and Wiley Interscience, New York; and Metzger et al. (1988) Nature, 334: 31-36. Many useful vectors for expression in bacteria, yeast, fungal, mammalian, insect, plant or other cells are well known in the art and may be obtained from commercial vendors or constructed de novo.

Knockout cassettes, vectors and other nucleic acids introduced into a host cell will likely contain a selectable marker, that is, a gene encoding a protein necessary for the survival or growth of a host cell transformed with the nucleic acid. Although such a marker gene may be carried on another polynucleotide sequence co-introduced into the host cell, it is most often contained on the transforming nucleic acid. Only those host cells into which the marker gene has been introduced will survive and/or grow under selective conditions. Typical selection genes encode proteins that (a) confer resistance to antibiotics or other toxic substances, e.g., hygromycin, ampicillin, neomycin, methotrexate, etc.; (b) complement auxotrophic deficiencies; or (c) supply critical nutrients not available from complex media. The choice of the proper selectable marker will depend on the host cell and appropriate markers for different hosts are well known in the art.

Selectable markers useful in practicing the methodologies of the invention disclosed herein can be “positive selectable markers”. Typically, positive selection refers to the case in which a genetically altered cell can survive in the presence of a toxic substance only if the recombinant polynucleotide of interest is present within the cell. For example, when a recombinant deletion cassette introduced into a cell contains a hygromycin B resistance gene, only those transformants containing the recombinant polynucleotide will survive when grown in the presence of hygromycin B. Other positive markers include, but are not limited to, mutated beta-tubulin (ben) gene, which confers resistance to benomyl; Bar, which confers resistance to phosphinothricin; Ble, which confers resistance to phleomycin; Sat-1, which confers resistance to nourseothricin, and cbx, conferring resistance to carboxin. Genes essential for the synthesis of an essential nutrient (such as amino acid arginine and nucleoside pyrimidine) may also be used as positive selection markers and are contemplated by the present invention. Negative selectable markers and screenable markers are also well known in the art and are contemplated by the present invention.

Screening and molecular analysis of recombinant strains of the present invention can be performed utilizing nucleic acid hybridization techniques. Hybridization procedures are useful for identifying polynucleotides, such as those modified using the techniques described herein, with sufficient homology to the subject regulatory sequences to be useful as taught herein. The particular hybridization techniques are not essential to the subject invention. As improvements are made in hybridization techniques, they can be readily applied by one of skill in the art. Hybridization probes can be labeled with any appropriate label known to those of skill in the art. Hybridization conditions and washing conditions, for example temperature and salt concentration, can be altered to change the stringency of the detection threshold. See, e.g., Sambrook et al. (1989) vide infra or Ausubel et al. (1995) Current Protocols in Molecular Biology, John Wiley & Sons, NY, N.Y., for further guidance on hybridization conditions.

Additionally, screening and molecular analysis of genetically altered strains, as well as creation of desired isolated nucleic acids can be performed using Polymerase Chain Reaction (PCR). PCR is a repetitive, enzymatic, primed synthesis of a nucleic acid sequence. This procedure is well known and commonly used by those skilled in this art (see Mullis, U.S. Pat. Nos. 4,683,195, 4,683,202, and 4,800,159; Saiki et al. (1985) Science 230:1350-1354). PCR is based on the enzymatic amplification of a DNA fragment of interest that is flanked by two oligonucleotide primers that hybridize to opposite strands of the target sequence. The primers are oriented with the 3′ ends pointing towards each other. Repeated cycles of heat denaturation of the template, annealing of the primers to their complementary sequences, and extension of the annealed primers with a DNA polymerase result in the amplification of the segment defined by the 5′ ends of the PCR primers. Since the extension product of each primer can serve as a template for the other primer, each cycle essentially doubles the amount of DNA template produced in the previous cycle. This results in the exponential accumulation of the specific target fragment, up to several million-fold in a few hours. By using a thermostable DNA polymerase such as the Taq polymerase, which is isolated from the thermophilic bacterium Thermus aquaticus, the amplification process can be completely automated. Other enzymes which can be used are known to those skilled in the art.

Hybridization-based screening of genetically altered strains typically utilizes homologous nucleic acid probes with homology to a target nucleic acid to be detected. The extent of homology between a probe and a target nucleic acid can be varied according to the particular application. Homology can be 50%-100%. In some instances, such homology is greater than 80%, greater than 85%, greater than 90%, or greater than 95%. The degree of homology or identity needed for any intended use of the sequence(s) is readily identified by one of skill in the art. As used herein percent sequence identity of two nucleic acids is determined using the algorithm of Karlin and Altschul (1990) Proc. Natl. Acad. Sci. USA 87:2264-2268, modified as in Karlin and Altschul (1993) Proc. Natl. Acad. Sci. USA 90:5873-5877. Such an algorithm is incorporated into the NBLAST and XBLAST programs of Altschul et al. (1990) J. Mol. Biol. 215:402-410. BLAST nucleotide searches are performed with the NBLAST program, score=100, wordlength=12, to obtain nucleotide sequences with the desired percent sequence identity. To obtain gapped alignments for comparison purposes, Gapped BLAST is used as described in Altschul et al. (1997) Nucl. Acids. Res. 25:3389-3402. When utilizing BLAST and Gapped BLAST programs, the default parameters of the respective programs (NBLAST and XBLAST) are used. See www.ncbi.nih.gov.

Preferred host cells are members of the genus Aureobasidium, especially A. pullulans. Filamentous fungi such as members of the genera Aspergillus, Trichoderma, Penicillium, etc. are also useful host organisms for expression of the DNA of this invention. (Van den Handel, C. et al. (1991) In: Bennett, J. W. and Lasure, L. L. (eds.), More Gene Manipulations in Fungi, Academic Press, Inc., New York, 397-428). Yeasts such as Saccharomyces cerevisiae, Candida albicans, Candida glabrata, and Cryptococcus neoformans, etc. are also useful host organisms.

Microbial Cultures

Aureobasidium pullulans is a ubiquitous fungus commonly found in samples of soil, water, air and decaying plant material. Isolates of A. pullulans exhibit polymorphic forms ranging from blastic conidia and swollen cells to pseudohyphae, hyphae, and chlamydospores, depending on isolate differences, age, medium and culture conditions (Cooke, Mycopathologia, 12:1-45 (1959); Leathers, Polysaccharides from eukaryotes. In: Vandamme, E. J., De Baets, S., and Steinbuchel, A., Editors. Biopolymers. Weinheim, Germany: Wiley-VCH. p. 1-35 (2002)). Most strains produce dark pigments (melanin) and pullulan, an exopolysaccharide that, in older cultures can lead to increased culture viscosity. Like most fungi, culture conditions under which A. pullulans is grown, affect multiple aspects of the biology of the organism, including morphological form and bioproduct spectrum.

Thus, one of skill in the art will recognize that multiple culture conditions can be modified in practicing the invention disclosed herein. Non-limiting examples of culture conditions that can be modified during the application and practice of the inventions disclosed herein, include: 1) temperature; 2) primary carbon source; 3) oxygen concentration; 4) primary nitrogen source; 5) pH; 6) mineral and other ion concentration; 7) age/growth phase of culture; 8) organization of an industrial fermenter; and 9) predominant morphological form. One of skill in the art will recognize that other culture parameters affecting desired bioproduct production and bioproduct yield can be modified.

In one aspect of the invention, cultures of A. pullulans strains described herein can be grown at any temperature that facilitates the production of one or more bioproducts. For example, a culture can be grown at a temperature of 15°−30° C., or any whole or partial degree within that range, including, but not limited to 15.0° C., 15.5° C., 16.0° C., 16.5° C., 17.0° C., 17.5° C., 18.0° C., 18.5° C., 19.0° C., 19.5° C., 20.0° C., 20.5° C., 21.0° C., 21.5° C., 22.0° C., 22.5° C., 23.0° C., 23.5° C., 24.0° C., 24.5° C., 25.0° C., 25.5° C., 26.0° C., 26.5° C., 27.0° C., 27.5° C., 28.0° C., 28.5° C., 29.0° C., 29.5° C., and 30.0° C.

In some embodiments, the microbial strains described herein can be grown under conditions where the pH of the culture facilitates the production of one or more bioproducts of interest. For example, a culture can be grown in media where the pH is between 5.5 and 8.5, 6.0 and 7.5, or any value within that range, including, but not limited to pH 5.5, 5.6, 5.7, 5.8, 5.9, 6.0, 6.1, 6.2, 6.3, 6.4, 6.5, 6.6, 6.7, 6.8, 6.9, 7.0, 7.1, 7.2, 7.3, 7.4, 7.5, 7.6, 7.7, 7.8, 7.9, 8.0, 8.1, 8.2, 8.3, 8.4, 8.5. One of skill in the art will recognize that a stable pH does not need to be maintained throughout the entirety of the growth of the strain producing the bioproduct(s) of interest. Thus, in some embodiments, the pH of a microbial culture of the present invention will vary. In other embodiments, pH buffers can be added to maintain a relatively stable pH where the pH of the culture medium over the life of the culture does not vary from a chosen starting point by more than ±0.5.

In some embodiments, microbial strains of the present invention can be grown in the presence of particular carbon sources. For example, a culture can be grown in the presence of simple carbon sources such as (D- or L-) arabitol, sucrose, fructose, glucose, mannose, galactose, arabinose, arabinose, xylose, mannitol, glucitol, galactitol, xylitol, ribitol, threitol, glycerol, gluconic acid, glucosamine, or meso-erythritol. Alternately, a culture can be grown in the presence of complex carbon sources such as cellulose, starch, beet molasses, carob pod, cornmeal hydrolysates, corn syrup, fuel ethanol fermentation stillage, grape skin pulp, vegetable oils, peat hydrolysate, hydrolyzed potato starch, and spent sulfite liquor. Carbon sources that are also sources for other nutritional requirements, such as nitrogen, can be utilized. For example, media for use in the present invention can include amino acids such as aspartate, threonine, lysine, methionine, isoleucine, asparagine, glutamic acid, glutamine, proline, alanine, valine, leucine, tryptophan, tyrosine, phenylalanine and their metabolic intermediates. These lists are non-limiting and it is well within the capabilities of one of skill in the art to utilize other carbon sources in practicing the present invention. Any carbon source can be used alone or in combination with other carbon sources.

Other nutritional parameters can also be varied, including nitrogen sources. Non-limiting examples of nitrogen sources include organic nitrogen sources (e.g., peptone, soybean pomace, yeast extract, food gravy, malt extract, corn steep liquor and soybean flour) and inorganic nitrogen sources (e.g, urea, ammonium sulfate, ammonium chloride, ammonium phosphate, ammonium carbonate and ammonium nitrate) can be included in growth media utilized in the practice of the present invention. Phosphate sources such as potassium dihydrogen phosphate, dipotassium hydrogen phosphate and their corresponding sodium-containing salts can be included in growth media as necessary. Metal and mineral salts such as salts of zinc, iron, magnesium, manganese, calcium and copper can be included as needed. Other nutritional supplements, such as vitamins (e.g, biotin, thiamine) can also be included. One of skill in the art will recognize that varying culture nutritional makeup can be utilized to maximize production of a bioproduct of interest and decrease production of undesired by-products. Any of these nutrients can be used alone or in combination with any other nutrient.

Nutrients can be added to the culture in any feeding regimen, including, but not limited to high cell-density culture, batch culture, fed-batch culture, constantly-fed-batch culture, exponentially-fed batch culture, continuous culture, or a mixture of these approaches for different nutrients.

In some instances, the length of time a culture is grown can be modified to enhance or begin production of a bioproduct of interest. For example, a culture can be grown for 10-300 hours, or more, or any time point within that range, for example 10, 20, 30, 40, 50, 60, 70, 80, 90, 100, 110, 120, 130, 140, 150, 160, 170, 180, 190, 200, 210, 220, 230, 240, 250, 260, 270, 280, 290, 300 hours, or more before harvesting of a bioproduct commences.

Additionally, optimization of bioproduct production can depend on growing a culture to a particular point in the life cycle. For example, a culture can be grown to early lag phase, middle lag phase, late lag phase, early exponential phase, mid-exponential phase, late exponential phase, early stationary phase, mid-stationary phase, or death phase. In some instances, cultures can be maintained in a growth phase (e.g., by fed-batch culture) in order to maintain a particular growth phase for the culture.

In other instances, culture conditions can be altered so that one morphological form of A. pullulans strains utilized to produce bioproduct(s) of interest predominates over other morphological forms. For example, culture conditions can be controlled so that yeast-like forms predominate, chlamydospores predominate, or hyphae/pseudohyphae predominate.

A. pullulans demonstrates strain-specific differences in bioproduct production and bioproduct production levels. Thus, in practicing the methodologies taught herein, a strain can be selected that already produces a bioproduct of interest, or produces a bioproduct of interest at a relatively higher level than other strains. One of skill in the art would be able to utilize the genetic alteration techniques described herein to produce an altered A. pullulans strain of differing genotypic/phenotypic backgrounds. Additionally, the approaches provided herein can be utilized to produce genetically altered species of the genus Aureobasidium other than A. pullulans that produce bioproducts of interest.

Bioproduct Extraction from Cultures

To utilize a bioproduct for downstream purposes (e.g., biofuel production or for use as a food additive), it may be necessary to extract the bioproduct of interest from the microbial culture. Given that bioproducts can comprise different chemical compounds with varying chemical properties, one of skill in the art will recognize that different approaches to isolate or purify a bioproduct from a microbial culture will necessarily need to be appropriate for that bioproduct.

A. pullulans produces numerous important bioproducts, including, but not limited to liamocins, pullulan, poly (β-malic acid), β-glucan, aureobasidin, and intracellular fatty acids or triacylglycerols. Although not all of these products are produced by every strain, many of these products are synthesized by A. pullulans NRRL 50384, however, the invention disclosed herein could be utilized with numerous other microorganisms as previously described. The technology for producing and isolating most Aureobasidium bioproducts are fairly well established, but alternative purification methods can be used depending on the desired applications. One of skill in the art will recognize that the following examples of extraction methodologies are provided as examples and are not meant to be limiting on the procedures that can be utilized to practice the invention disclosed herein.

Pullulan and poly(β-L-malic acid) (PMA) are predominantly extracellular and isolated from cell-free culture supernatants. Pullulan and PMA are water soluble, thus are typically isolated from cultures by collecting supernatants and precipitating the bioproducts. One approach to isolating these products was described by Manitchotpisit et al. (ibid., 2012). Cells were removed by centrifugation at 10,000×g for 20 min. The culture supernatants were adjusted to pH 5.0 by the dropwise addition of 30% (w/v) CaCO₃. Pullulan was precipitated by the addition of one volume of 95% ethanol followed by centrifugation at 16,900×g for 30 min. PMA was then precipitated by the addition of an additional volume of 95% ethanol, followed by incubation at 4° C. overnight and centrifugation at 16,900×g for 30 min. Precipitated PMA was dissolved in 200 mL of purified water and lyophilized. Any other isolation methodology appropriate for these bioproducts can be utilized.

Liamocins are typically extracellular and can be separated by centrifugation and purified through solvent extraction. The following example is from Manitchotpisit et al. (ibid. 2011). Approximately 50 ml of cells and heavy oil were removed by centrifugation at 10,000×g for 20 min. Extracellular heavy oil appeared as a layer beneath the precipitated cells. Cells were gently resuspended in 3-5 ml of distilled water and transferred to a screw-cap glass tube (13 mm×100 mm). Culture flasks and centrifuge bottles were washed with 3-5 ml of methyl ethyl ketone and heavy oil was dissolved in this solvent. The dissolved oil was recombined with the resuspended cells and the mixture was vortexed vigorously and allowed to separate overnight at room temperature. The aqueous and extracted cell layers were then removed, and the solvent was evaporated from the oil overnight under a stream of air. Alternatively, whole cultures were extracted with at least 50 ml of methyl ethyl ketone, and solvent, aqueous, and biomass layers were isolated in a separatory funnel. The whole culture method is simpler but requires more solvent and more time for solvent evaporation.

A number of studies describe additional (non-pullulan) polysaccharides, typically water-soluble extracellular polysaccharides, including certain β-glucans, from certain strains and mutants of A. pullulans (Leathers, Polysaccharides from eukaryotes. In: Vandamme, E. J., De Baets, S., and Steinbuchel, A., Editors. Biopolymers. Weinheim, Germany: Wiley-VCH. p. 1-35 (2002)). A typical purification of β-glucans can involve removing cells by centrifugation or filtration, removing contaminants by adsorption with activated carbon, concentrating polysaccharides by ultrafiltration, and precipitating final product with 80% ethanol (Muramatsu, et al., PLoS One, 7:(2012)).

Aureobasidins are typically extracellular and purified from a fermentation broth through solvent extraction and column purification. A typical purification could involve solubilizing aureobasidins in fermentation broth with an equal volume of ethanol, separating on an adsorption column (e.g., a Diaion HP-40 column) equilibrated with 50% ethanol and eluted with 95% ethanol, diluting elute twice with water and further separating on reverse phase ODS-W (Soken ODS-W from Soken Chemicals Co.) equilibrated with 40% ethanol and eluted with 60% ethanol (Yoshikawa, et al., J. Antibiotics (Tokyo), 46:1347-54 (1993)).

Triacylglycerol or triglycerides are typically intracellular and removed from cells through solvent extraction. A number of different solvent extraction methods allow preferential solubilization of the desired lipid (Christie, Advances in Lipid Methodology, 5:97-115 (2003)). These solvent extraction methods can be utilized with dried (i.e., lyophilized, oven) cultures or cells that have been lysed through mechanical, chemical, or enzymatic processes (Yu, et al., Eur. J Lipid Sci. Tech., 117:730-737 (2015)). A typical extraction method for A. pullulans would involve collecting cells through centrifugation, washing with saline, drying at 80° C., and homogenizing cells with 2:1 chloroform-methanol mixture.

Massoia lactone production by A. pullulans has never been reported or demonstrated prior to our construction of a strain lacking a functional PKS gene. During analysis of that knockout strain, we discovered that massoia lactone can be found in the extracellular liamocin fractions and intracellularly for A. pullulans. Massoia lactone can be separated directly from liamocins by butan-2-one:chloroform:water (1:2:2 by volume) partitioning. Alternatively, massoia lactone can be extracted from lysed cells of this knockout strain using chloroform:methanol (1:1) or acetone:ethyl acetate (1:1), but further purification is required.

Bioproducts and Uses

In practicing the present invention, it will be recognized by one of skill in the art that any of the disclosed strains can be utilized to produce a bioproduct of interest. In some instances, an A. pullulans strain lacking at least one gene encoding a mannitol biosynthetic enzyme (See, FIG. 2) can be utilized to produce a bioproduct of interest. In some embodiments, the present invention can be practiced using an A. pullulans strain lacking a functional mannitol-1-phosphate-dehydrogenase-encoding (MPD1) gene (SEQ ID NO. 1) to produce a bioproduct of interest. In another embodiment, the present invention can be practiced using an A. pullulans strain lacking a functional mannitol-dehydrogenase-encoding (MDH2) gene (SEQ ID NO. 3) to produce a bioproduct of interest. In another embodiment, the present invention can be practiced using an A. pullulans strain lacking a functional polyketide-synthase-encoding (PKS) gene (SEQ ID NO. 4) to produce a bioproduct of interest. In some embodiments, the present invention can be practiced using an A. pullulans strain lacking a functional putative-mannitol-dehydrogenase-encoding (MDH1) gene (SEQ ID NO. 2) to produce a bioproduct of interest. In still another embodiment, the present invention can be practiced using an A. pullulans strain lacking a functional MPD1 gene and lacking a functional PKS gene to produce a bioproduct of interest. In still another embodiment, the present invention can be practiced using an A. pullulans strain lacking a functional MDH2 gene as well as lacking a functional PKS gene to produce a bioproduct of interest, while not producing melanin. In still another embodiment, the present invention can be practiced using an A. pullulans strain lacking a functional MPD1 gene, lacking a functional MDH2 gene, and lacking a functional PKS gene to produce a bioproduct of interest, while not producing melanin. In particular embodiments, one of the strains described in the Examples section can be utilized to produce a bioproduct of interest. In other embodiments, the present invention can be practiced using an A. pullulans strain lacking a functional copy of a combination of any or all genes (MDH1, MDH2, MPD1, PKS) described herein.

Liamocins

Experiments utilizing Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry (MALDI-TOF MS) spectra suggested that extracellular oil produced by A. pullulans oil contained a family of related oil structures. The structure of several of the oil components (termed “liamocins”) from A. pullulans strain NRRL 50380 have previously been elucidated (Price et al., Carbohyd. Res., 370:24-32 (2013)). The liamocins identified to date are comprised of a polyol head group (either mannitol, arabitol, or glycerol) that is ester-linked at one end to a highly unusual fatty acid, 3,5-dihydroxydecanoic acid (FIG. 1). These 3,5-dihydroxydecanoic acid groups are themselves joined by 1,5-linked ester bonds, so that the liamocins form either A, B, or C-type that contain three, four, or five 3,5-dihydroxydecanoic acid groups, respectively. In addition, some liamocins contain a single 3′-O-acetyl group at the free 3-hydroxy position on the 3,5-dihydroxydecanoic fatty acid chain. Liamocins A1 and B1 are non-acetylated, whereas A2 and B2 each contain a single acetyl group.

Analysis of numerous liamocin-producing A. pullulans isolates grown under varying conditions reveal that liamocin trimers with a mannitol headgroup (e.g., Man-A1, Man-A2) are usually the predominant structure when glucose, fructose, sucrose, or xylose are used as the carbon source. Some A. pullulans strains have been identified that produced liamocins that were approximately 40% arabitol-containing structure (e.g., Ara-A1, Ara-A2, Ara-B1) when grown on glucose. Prior to the inventions disclosed herein, however, 100% arabitol-containing liamocin structures could only be produced by growing cells using arabitol as the sole carbon source. This method likely would be cost-prohibitive for many applications because of the relative expense of arabitol compared with glucose. Additionally, separating mixed liamocin structures (e.g., combinations of mannitol-liamocin and arabitol-liamocin) is technically very difficult. Thus, the strains and methodologies disclosed herein that modify the synthesis and/or accumulation of intracellular polyols in genetically altered Aureobasidium strains of the present invention would be valuable as a method to alter the chemical structures of the liamocins and to decrease unwanted polyol synthesis as contaminants of other bioproducts of interest.

Thus, in one embodiment, arabitol-liamocins can be produced utilizing an A. pullulans strain of the invention when grown in the absence of arabitol as a carbon source. In some embodiments, the A. pullulans strain utilized to produce arabitol-liamocins lacks at least one gene in a mannitol biosynthetic pathway. In other embodiments, an A. pullulans strain lacking a functional gene encoding mannitol-1-phosphate dehydrogenase (MPD1) has been is utilized to produce arabitol-liamocins. In still another embodiment, an A. pullulans strain lacking a functional MPD1 gene and lacking a functional MDH2 gene is utilized to produce arabitol-liamocins.

For example, any strains lacking one or more genes encoding for any protein necessary for mannitol production can be grown in the presence of D-fructose, D-glucose, D-mannose, D-galactose, D-arabinose, L-arabinose, D-xylose, D-mannitol, D-glucitol, D-galactitol, D-xylitol, D-ribitol, D-threitol, L-threitol, D-glycerol, or meso-erythritol. One of skill in the art will recognize that this list of carbon sources is not exclusive and that any carbon source that results in production of the desired bioproduct can be utilized. In a particular embodiment, the inexpensive carbon source, D-glucose can be utilized to produce arabitol-liamocins utilizing any the strains of this invention. In another particular embodiment, arabitol-liamocins are produced utilizing any of the knockout strains described in the Examples below.

In still other embodiments of the present invention, A. pullulans strains lacking at least one gene encoding a mannitol biosynthetic enzyme as well as lacking a gene encoding polyketide synthase (PKS) are used to produce liamocins that are melanin-free. In one embodiment, a strain used to produce melanin-free liamocins lacks a functional MPD1 gene and lacks a functional PKS gene. In another embodiment, a strain used to produce melanin-free liamocins lacks a functional MDH2 gene and lacks a functional PKS gene. In still another embodiment, a strain used to produce melanin-free liamocins lacks a functional MPD1 gene, lacks a functional MDH2 gene, and lacks a functional PKS gene. In particular embodiments, a specific strain described in the Examples below can be utilized to produce arabitol-liamocins that are essentially free of melanin without the need to remove melanin.

The strains described herein comprising one or more genetic alterations can be used to produce a desired liamocin. In one embodiment, D- and/or L-mannitol liamocin A1, D- and/or L-mannitol liamocin A2, D- and/or L-mannitol liamocin B1, D- and/or L-mannitol liamocin B2, D- and/or L-mannitol liamocin C1, or D- and/or L-mannitol liamocin C2, or a combination thereof, can be produced as a bioproduct utilizing the strains of this invention. In another embodiment, D- and/or L-arabitol liamocin A1, D- and/or L-arabitol liamocin A2, D- and/or L-arabitol liamocin B1, D- and/or L-arabitol liamocin B2, D- and/or L-arabitol liamocin C1, or D- and/or L-arabitol liamocin C2, or a combination thereof, can be produced as a bioproduct utilizing the strains of this invention. In a third embodiment, 2-amino-D-mannitol liamocin A1, 2-amino-D-mannitol liamocin A2, 2-amino-D-mannitol liamocin B1, 2-amino-D-mannitol liamocin B2, 2-amino-D-mannitol liamocin C1, or 2-amino-D-mannitol liamocin C2, or a combination thereof, can be produced as a bioproduct utilizing the strains of this invention. In a fourth embodiment, 2-N-acetylamino-D-mannitol liamocin A1, 2-N-acetylamino-D-mannitol liamocin A2, 2-N-acetylamino-D-mannitol liamocin B1, 2-N-acetylamino-D-mannitol liamocin B2, 2-N-acetylamino-D-mannitol liamocin C1, or 2-N-acetylamino-D-mannitol liamocin C2, or a combination thereof, can be produced as a bioproduct utilizing the strains of this invention. In a fifth embodiment, D-fucitol liamocin A1, D-fucitol liamocin A2, D-fucitol liamocin B1, D-fucitol liamocin B2, D-fucitol liamocin C1, or D-fucitol liamocin C2, or a combination thereof can be used as the antibacterial compound of this invention. In a sixth embodiment, L-rhamnitol liamocin A1, L-rhamnitol liamocin A2, L-rhamnitol liamocin B1, L-rhamnitol liamocin B2, L-rhamnitol liamocin C1, L-rhamnitol liamocin C2, or a combination thereof can be produced as a bioproduct utilizing the strains of this invention. In a seventh embodiment, L-glycerol liamocin A1, L-glycerol liamocin A2, L-glycerol liamocin B1, L-glycerol liamocin B2, L-glycerol liamocin C1, L-glycerol liamocin C2, D-glycerol liamocin A1, D-glycerol liamocin A2, D-glycerol liamocin B1, D-glycerol liamocin B2, D-glycerol liamocin C1, D-glycerol liamocin C2, L-threitol liamocin A1, L-threitol liamocin A2, L-threitol liamocin B1, L-threitol liamocin B2, L-threitol liamocin C1, L-threitol liamocin C2, D-threitol liamocin A1, D-threitol liamocin A2, D-threitol liamocin B1, D-threitol liamocin B2, D-threitol liamocin C2, L-erythritol liamocin A1, L-erythritol liamocin A2, L-erythritol liamocin B1, L-erythritol liamocin B2, L-erythritol liamocin C1, L-erythritol liamocin C2, D-erythritol liamocin A1, D-erythritol liamocin A1, D-erythritol liamocin B1, D-erythritol liamocin B2, D-erythritol liamocin C1, D-erythritol liamocin C2, or a combination thereof can be produced as a bioproduct utilizing the strains of this invention. In still another embodiment, a fructose liamocin (FIG. 13) and exophilins can be produced by a strain of the present invention lacking functional MPD1 and MDH1 genes. In yet another embodiment, any combination of any of the compounds (glycerol-liamocins, threitol-liamoicins, erythritol-liamocins, mannitol-liamocins, arabitol-liamocins, 2-amino-D-mannitol liamocins, 2-N-acetylamino-D-mannitol liamocins, D-fucitol liamocins, fructose-liamocins and L-rhamnitol liamocins) mentioned in this paragraph can be produced as a bioproduct utilizing the strains of this invention.

In another embodiment, a liamocin produced is any of the compounds described in Formula 1 where R₁ is either, independently, COCH₃ or H; and R₂ is, independently, one or more O-linked 3,5-dihydroxy-decanoate groups; and R₃ is, independently, C_(x)O_(x)H_(2x+1), such as one of the following: L- or D-glycerol, L- or D-threitol, L- or D-erythritol, L- or D-arabitol, L- or D-xylitol, L- or D-lyxitol, L- or D-ribitol, L- or D-allitol, L- or D-altritol, L- or D-mannitol, L- or D-iditol, L- or D-gulitol, L- or D-glucitol (also called sorbitol), L- or D-galactitol (also called dulcitol), L- or D-talitol, 2-amino-D-mannitol, 2N-acetylamino-D-mannitol, L-rhamnitol, or D-fucitol; individually or in combination with each other, can be produced as a bioproduct utilizing the strains of this invention. In still another embodiment, any or all of the above liamocins can be produced as a bioproduct by a strain of this invention that lacks the ability to produce melanin. Thus, in such embodiments, liamocins that are essentially free of melanin are produced by growing strains lacking a functional PKS gene under conditions sufficient to produce the desired liamocin. In a particular embodiment, a desired liamocin is produced by a PKS knockout strain produced by the methods described in the Examples below.

Pullulan

A well-established product of A. pullulans is the exopolysaccharide, pullulan. This complex polysaccharide is a linear homopolysaccharide of glucose that is often described as an α-(1→6) linked polymer of maltotriose subunits, however, other structures (such as the tetramer maltotetraose) may be present within a pullulan polymeric chain (Leathers, Polysaccharides from eukaryotes. In: Vandamme, E. J., De Baets, S., and Steinbuchel, A., Editors. Biopolymers. Weinheim, Germany: Wiley-VCH. p. 1-35 (2002)). Regular alternation of the (1→4) and (1→6) bonds results in two distinctive properties of this large molecule, namely, structural flexibility and enhanced solubility (Leathers, 1993). Pullulan also demonstrates adhesive properties and a capacity to form fibers, compression moldings and strong, oxygen-impermeable films. Chemical derivatization utilizing reactive groups can be used to alter the solubility (and other physiochemical properties) of pullulan. Pullulan is non-toxic, edible, and biodegradable, making it useful in a wide variety of industrial applications, pharmaceutical applications and food applications.

Pullulan is considered a dietary fiber in humans and provides few calories because it is resistant to mammalian amylases. Some studies indicate that it functions as a prebiotic, promoting the growth of beneficial bacteria. Pullulan can be incorporated in both solid and liquid foods, where it functions to achieve desired consistency, dispersability, moisture retention, and other parameters. It can be used as a replacement for starch in multiple food applications. It can also serve as a food preservative, as pullulan is not readily assimilated by the bacteria and fungi responsible for food spoilage. It has adhesive properties, making it useful as a binder and stabilizer in food pastes.

Films made of pullulan are clear, oxygen-permeable and dissolve readily in water, thus, these films readily melt in the mouth. One of the primary uses of such films is in the oral care industry, where pullulan film is impregnated with mouthwash or other oral hygiene products. Pullulan films can also be used as coating or packaging material for dried foods, or applied directly to food as a protective coating.

In the pharmaceutical industry, pullulan can be used as a coating or layer for tablets, pills, and granules. It can be utilized as both a coating in slow-release formulations as well as a preservative to prevent color and taste changes. Pullulan also shows promise as a conjugate for vaccines and can be used as a blood plasma expander in place of dextran.

Pullulan finds use in the cosmetics industry because it is non-toxic and non-irritating to the human body. Eye cosmetics, lotions and shampoos, as well as powders, facial packs, hair dressings and tooth powders can all contain pullulan.

Pullulan can also be formed into fibers that resemble nylon or rayon. Pullulan that is compressed or extruded can be formed into materials that resemble polystyrene or polyvinyl alcohol. Pullulan also has applications in a wide variety of industries, from making paint and electronics components to paper production and use as a flocculating agent.

However, pullulan is expensive to make, despite its ecological benefits over petroleum products. One impediment to producing pullulan is the need to extract melanin and melanin-related pigments which contaminate cultures of A. pullulans. Thus, one object of the present invention is to provide A. pullulans strains that make pullulan more economically feasible by, for example, bypassing the step of removing melanin, which adds extra time and expense to the pullulan production process.

In one embodiment, the present invention provides a method of producing melanin-free pullulan directly in cultures of A. pullulans. This embodiment can be achieved by utilizing a strain lacking a functional PKS gene. In a particular embodiment, production of melanin-free pullulan directly in a culture is achieved using a strain specifically disclosed in the Examples section below.

Massoia Lactone

Massoia lactone is an alkyl lactone derived from the bark of the Massoia tree (Cryptocaria massoia) found in Papua, Indonesia. Massoia lactone is a popular natural coconut flavoring ingredient, but harvesting and extracting this compound from the bark of the Massoia tree is an expensive process that results in death of the tree. Consequently, most massoia lactone is synthetically produced from petroleum-based precursors, despite consumer and producer preferences for natural products (Harbindu and Kumar, Synthesis (12):1954-59 (2011). Prior to construction of the PksKO strain described herein, there has never been a report or other description of a massoia-lactone-producing strain of A. pullulans. Thus, we describe herein an invention allowing the production of massoia lactone by A. pullulans. A. pullulans represents a potential alternative source of massoia lactone that is natural, renewable, and environmentally friendly. In addition, we anticipate that the market size of massoia lactone could increase significantly if we are able to reduce the cost through fermentative production. In addition, there may be other potential applications of using massoia as an anti-bitter agent for artificial sweeteners (Putter and Wonschik, PCT Pub. No. WO2013079187) and also an oxygenate fuel additive (Robinson, US. Pub. No. US20060096158A1).

Production of massoia lactone by Aureobasidium species, including A. pullulans, has not been previously described. Thus, one embodiment of the present invention is a massoia-lactone-producing strain of A. pullulans. Another embodiment of the present invention is a strain of A. pullulans that lacks a functional PKS gene. Still another embodiment of the present invention is a massoia-lactone-producing strain of A. pullulans that lacks a functional PKS gene and also lacks one or more of: a functional MPD1 gene, a functional MDH2 gene, and a functional MDH1 gene.

Other Bioproducts

One of skill in the art will recognize that the strains of A. pullulans described herein can be used to produce a bioproduct of interest. In some embodiments, the bioproduct produced utilizing the strains and methods of the present invention is a liamocin, pullulan or massoia lactone. In other embodiments, the bioproduct produced utilizing the strains and methods of the present invention is poly (β-malic acid), β-glucan, aureobasidin, a lactone, an intracellular fatty acid or triacylglycerol. In still other embodiments, a strain of A. pullulans that lacks a functional PKS gene and is grown under conditions sufficient to produce one or more melanin-free bioproducts, including but not limited to a liamocin, pullulan, massoia lactone and other lactones, poly (β-malic acid), β-glucan, aureobasidin, an intracellular fatty acid and triacylglycerol.

Products

The present invention further provides a medicament, nutritional or pharmaceutical composition comprising any of the bioproducts produced by a genetically altered strain of the present invention. These compositions can be administered in various ways suitable for therapy and can be administered alone or as an active ingredient in combination with pharmaceutically acceptable carriers, diluents, adjuvants, and vehicles. Conventional methods such as administering the compounds as tablets, suspensions, solutions, emulsions, capsules, powders, syrups, and the like are usable. Known techniques to deliver the compositions orally or intravenously and retain biological activity are preferred. Formulations that can be administered subcutaneously, topically, or parenterally or intrathecal and infusion techniques are also contemplated by the present invention as well as suppositories and implants.

Pharmaceutically acceptable carriers, diluents, adjuvants and vehicles as well as implant carriers generally refer to inert, non-toxic solid or liquid fillers, diluents, or encapsulating material not reacting with the active ingredients of the invention. The pharmaceutical formulations suitable for injection include sterile aqueous solutions or dispersions and sterile powders for reconstitution into sterile injectable solutions or dispersions. The carrier can be a solvent or dispersing medium containing for example, water, ethanol, polyol such as glycerol propylene glycol, liquid polyethylene glycol, etc., and suitable mixtures thereof and vegetable oils.

Proper fluidity can be maintained by the use of a coating such as lecithin, by the maintenance of the required particle size in the case of dispersion and by the use of surfactants. Nonaqueous vehicles such as cottonseed oil, sesame oil, olive oil, soybean oil, corn oil, sunflower oil, or peanut oil and esters, such as isopropyl myristate, may also be used as solvents for compound compositions. Additionally various additives which enhance the stability, sterility, and isotonicity of the compositions, including antimicrobial preservatives, antioxidants, chelating agents, and buffers, can be added. Prevention of the action of microorganisms can be ensured by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, sorbic acid, etc. It may be desirable to include isotonic agents, for example sugars, sodium chloride, etc. Prolonged absorption of the injectable pharmaceutical form can be brought about by the use of agents delaying absorption, for example, aluminum monostearate, gelatin, etc. Any vehicle, diluents or additive used would have to be compatible with the anti-microbial adhesion fraction A6 of the invention. The choice of delivery system is well within the ordinary skill in the art.

Having described the invention in general, below are examples illustrating the generation and efficacy of the invention. Neither the examples, nor the general description above should be construed as limiting the scope of the invention.

EXAMPLES Example 1

A hygromycin expression cassette used in these transformations was constructed by fusing an A. pullulans trans-elongation factor (TEF) promoter to an Escherichi coli hygromycin phosphotransferase gene. This was accomplished by PCR amplification of the TEF promoter using degenerate oligonucleotides ApTEF-F and ApTEF-R (Table 1); and A. pullulans NRRL 50383 (RSU6) DNA as template. The product was then cloned into pCR2.1 (Invitrogen) and further modified by PCR amplification with primers ApTEF-Sal1 and ApTEF-EcoRV in order to introduce restriction endonuclease sites. Plasmid pCSN43 was also modified by removing the 0.3 kb Xbal fragment and re-ligating the remaining 5.0 kb plasmid in order to shorten the A. nidulans TrpC terminator and remove an adjacent Cla1 site within the polylinker. The A. nidulans TrpC promoter was then removed from this resultant plasmid by cutting with Cla1, blunting the restriction endonuclease overhangs, and then digesting with Sal1. This linear fragment was then ligated to the modified TEF promoter fragment digested with Sal1 and EcoV. Lastly, this modified plasmid was used as template for PCR amplification with primers TEF-Hyg-P1 and TEF-Hyg-P2. This 2.5 kb hygromycin resistance cassette was used for all further plasmid constructs.

TABLE 1 Primers SEQ Primer ID name Sequence 5′ → 3′ NO. ApTEF-F ( GGCTAGRYGCRCGAYTATYCAC 8 ApTEF-R GTTGACGGTKRTGTATGGAAG 9 ApTEF-SalI GCAGGTCGACGGCTAGGCGCGCGATTATTC 10 ApTEF-EcoRV GCAGGATATCTTGACGGTTGTGTATGGAAGATTGAG 11 TEF-Hyg-P1 CGGCTAGGCGCGCGATTATTC 12 TEF-Hyg-P2 CGGCCGGCGTATTGGGTGTTA 13 pUC18-P1 CGTAATCATGGTCATAGCTGTTTCC 14 pUC18-P2 GCACTGGCCGTCGTTTTACAA 15 Mpd-P1Gib GTCACGACGTTGTAAAACGACGGCCAGTGCGACCCG 16 CCGCTCTTTGACCTACAG Mpd-P2Gib GCTGTGAATAATCGCGCGCCTAGCCGGGAGGGGAAC 17 AAAGCCATCACACC Mpd-P3Gib GCTCCGTAACACCCAATACGCCGGCCGGCGTGTCGG 18 TCGTGCTCCTCTC Mpd-P4Gib CACACAGGAAACAGCTATGACCATGATTACGTTGTG 19 GGGCTTTGGAATCTGTGGA Mpd-P5 GCGGCAACATCGGTCGTGG 20 Mpd-P6 CATTCCTTGCCGCGGTTGTAG 21 Mpd-P7 TCAAGCGCCAAGGTTATCGGTCTG 22 Hyg-P11 GCCGCTTTCCCTCCCATTCC 23 Mpd-P8 GTGGCGACGATGGAGGCTTCT 24 Hyg-P13 AGCCCCTGGGTTCGCAAAGATAAT 25 PKS4-P1Gib GTCACGACGTTGTAAAACGACGGCCAGTGCGGCTTT 26 GGGCGCATACCGAGAG PKS4-P2Gib GCTGTGAATAATCGCGCGCCTAGCCGGCTGAAGGCC 27 AGCACATCCAACT PKS4-P3Gib GCTCCGTAACACCCAATACGCCGGCCGGTCGGCCAG 28 CGCATCCTCGTAT PKS4-P4Gib CACACAGGAAACAGCTATGACCATGATTACGGCTTC 29 CTCCTGCTGCCAACACTC PKS4-P5 TCAGGGCCGATGTTAGGGATGCT 30 Hyg-P10 TCGGCAGGATATCTTGACGGTTGT 31 PKS4-P6 GTCCCGCCGGCTGTAAGGTG 32 Hyg-P13 AGCCCCTGGGTTCGCAAAGATAAT 33 PKS4-P7 GCGAGCGAGAGCGACCTGGAT 34 PKS4-P8 ACAACTTCTCCGCTGCTGGTGGTAA 35 PKS4-P1 GGCTTTGGGCGCATACCGAGAG 36 PKS4-P4 GCTTCCTCCTGCTGCCAACACTC 37 MPD1-P1 GACCCGCCGCTCTTTGACCTACAG 38 MPD1-P4 TTGTGGGGCTTTGGAATCTGTGGA 39 Hyg-P1 AGCTGCGCCGATGGTTTCTACAA 40 Hyg-P2 CTGGGGCGTCGGTTTCCACTATC 41 Ura3-P1Gib GTCACGACGTTGTAAAACGACGGCCAGTGCCGCCGC 42 GTGCTTCCGTAGA Ura3-P5Gib GGTGCGTTGATGGTGCTGATCCTCTTCCTGGATACA 43 TCGGCCGAAACACAG Ura3-P4Gib CACACAGGAAACAGCTATGACCATGATTACGGTAGG 44 CGTATGCTGGTGGTGTTGG Ura3-P6Gib GGAAGAGGATCAGCACCATCAACGCACCGAGCAGCG 45 CGGGTAATTTGATGAC Ura3-P1 CGCCGCGTGCTTCCGTAGA 46 Ura3-P4 GTAGGCGTATGCTGGTGGTGTTGG 47 Ura3-P7 TGGGGTGAGGGAAAGAGAAGGACA 48 Ura3-P8 CGCTCAAAGGGCAAACATCAAAGA 49 Mdh1-P1Gib GTCACGACGTTGTAAAACGACGGCCAGTGCTGCGGA 50 GCCAACACCCAGATAG Mdh1-P2Gib GAACTTGTCCTTCTCTTTCCCTCACCCCAGGAAGCC 51 ACCGACACCAATGTG Mdh1-P3Gib GGATCTTTGATGTTTGCCCTTTGAGCGACTTCCGCC 52 GTCTCTGTTTCGTC Mdh1-P4Gib CACACAGGAAACAGCTATGACCATGATTACGGAGGC 53 TGAGGACAAGGCAAGAGAT Mdh1-P1 TGCGGAGCCAACACCCAGATAG 54 Ura3-P13 CACGGCGGTATTGAGCGAGGTAA 55 Mdh-P4 GAGGCTGAGGACAAGGCAAGAGAT 56 Ura3-P15 GCCGCAAAGCAGACGAACCT 57 Mdh2-P1Gib GTCACGACGTTGTAAAACGACGGCCAGTGCGAGTGG 58 GCGGAGTTGGCGATAG Mdh2-P2Gib GAACTTGTCCTTCTCTTTCCCTCACCCCAAGCGGCC 59 TCAATACCCATACCAC Mdh2-P3Gib GGATCTTTGATGTTTGCCCTTTGAGCGCTCTGACGC 60 CTCCACCTACACCAC Mdh2-P4Gib CACACAGGAAACAGCTATGACCATGATTACGTTCAC 61 CCTTCGCCCAAACTGC Mdh2-P1 GAGTGGGCGGAGTTGGCGATAG 62 Mdh2-P2 TTCACCCTTCGCCCAAACTGC 63

Example 2

MPD1 Disruption Cassette/Strain Construction

A MPD1 (SEQ ID NO. 1) disruption plasmid was constructed by Gibson assembly using the following PCR fragments: (1) pUC18 amplified with primers pUC18-P1 and pUC18-P1, (2) MPD1 5′ region amplified with primers MPD-P1 Gib and MPD-P2Gib, (3) MPD1 3′ region amplified with primers MPD-P3Gib and MPD-P4Gib, and (4) the 2.5 kb hygromycin resistance cassette previously amplified with primers TEF-Hyg-P1 and TEF-Hyg-P2 (FIG. 3) (See, Table 1 for primer sequences). The resultant plasmid served as template for PCR amplification of the overlapping split marker regions using primer combinations, a) MPD1-P1 and Hyg-P2; and b) MPD1-P4 and Hyg-P1. The resulting PCR product formed the MPD knockout cassette (SEQ ID NO. 6). The DNA fragments were purified by column separation or ethanol precipitation; and then used in equimolar amounts for transformation of A. pullulans NRRL 50384. Transformation was carried using electroporation as previously described (Varma, et al., Infect. Immun., 60(3):1101-8 (1992)) using logarithmically growing cells. After electroporation, cells were recovered for 3 hr in YPD medium (1% YE, 2% peptone, 2% glucose) prior to plating on YPD-Hyg plates containing 100 μg/ml hygromycin B.

Isolates were transferred at least two times on YPD-Hyg plates and then screened by PCR amplification to confirm the following integration patterns: (1) deletion of the native mpd1 gene using primers Mpd-P5 and Mpd-P6, (2) 5′ cross-over integration of the transforming DNA using Mpd-P7 and Hyg-P11, and (3) 3′ cross-over integration of the transforming DNA using Mpd-P8 and Hyg P13 (See, Table 1 for primer sequences). Primers Mpd-P7 and Mpd-P8 both anneal outside of the homologous regions of the transforming DNA so PCR amplification as described is persuasive evidence of gene replacement as designed.

Example 3

The isolated MPD1 knock-out (MpdKO) transformants and parent strain A. pullulans NRRL 50384 were grown overnight in complex medium supplemented with either 50 g/L glucose or 50 g/L fructose. Cells were then harvested, lysed by shaking with 0.5 mM zirconia/glass beads, and centrifuged to produce cell-free lysate. These lysates were then analyzed for mannitol, arabitol, glycerol, and trehalose content by HPCL using an Aminex HPX-87H column and refractive index for detection. All polyol and trehalose concentrations were normalized against the protein content to normalize for discrepancies in lysis efficiency. The MpdKO strain produced approximately 12× less intracellular mannitol compared with A. pullulans NRRL 50384 when grown on glucose. The results are shown in Table 2, where standard deviations are in parentheses and values with statistically different values compared with NRRL 50384 controls grown under the same condition are marked with asterisks (p<0.05 with T-Test). Under these same conditions, there was almost a 2-fold increase in glycerol and 35% increase in trehalose for the MpdKO strain compared with the parent isolate. However, there was not any statistical difference in the amount of intracellular arabitol with this group. When this same strain were grown with fructose, there was not any statistical difference for the intracellular polyols and trehalose between the NRRL 50384 and MpdKO strain, but there were large differences in relative amounts compared with NRRL 50384 grown in glucose. Most notable was the 4-fold increase in mannitol for NRRL 50384 when grown in fructose containing medium. It is assumed the increased mannitol is due to fructose being converted directly into mannitol through a Mdh2-mediated reaction. This reaction would explain why the MpdKO strain did not exhibit decreased mannitol when grown with fructose, since Mpd1 protein would not be involved in this pathway (FIG. 2).

TABLE 2 Polyol and Trehalose Accumulation in WT and MpdKO strains. Relative intracellular concentrations Strain/carbon source Mannitol Arabitol Glycerol Trehalose 50384/glucose 0.660 (0.020) 0.127 (0.021) 0.062 (0.001) 2.070 (0.022) MpdKO/glucose  0.055 (0.014)* 0.109 (0.011)  0.112 (0.015)*  2.801 (0.156)* 50384/Fructose 2.768 (0.046) 0.012 (0.021) 0.038 (0.016) 0.323 (0.008) MpdKO/fructose 2.7196 (0.107)  0.028 (0.010) 0.028 (0.010) 0.323 (0.010)

Example 4 ((MpdKO Strain, Liamocin Analysis))

To analyze whether deletion of the MPD1 gene shifted bioproduct production in genetically altered A. pullulans strains, liamocins were produced and purified as previously described (Manitchotpisit, 2011, ibid.) from cultures grown with 50 g/L glucose, the MpdKO strain produced nearly 100% arabitol-containing liamocins compared to 100% mannitol-containing liamocins for NRRL 50384 (FIG. 4). Under these conditions, there was only a 15% decrease in yield compared with the wildtype, demonstrating that the robustness and productivity of this strain were minimally affected. When grown with 50 g/L fructose, there was not any statistical difference in liamocin yield and molecular structures between the parent and MpdKO strains (FIG. 5). It is assumed that the formation of mannitol-containing liamocins under these conditions is a result of the high amount of mannitol, presumably from mannitol dehydrogenase (the protein encoded by MDH2) conversion of fructose, and the relatively lower amount of arabitol.

Example 5

PKS Disruption Cassette/Strain Construction

A PKS4 disruption plasmid was constructed by Gibson assembly using the following PCR fragments: (1) pUC18 amplified with primers pUC18-P1 and pUC18-P1, (2) PKS4 5′ region amplified with primers PKS4-P1Gib and PKS4-P2Gib, (3) PKS4 3′ region amplified with primers PKS4-P3Gib and PKS4-P4Gib, and (4) the 2.5 kb hygromycin resistance cassette previously amplified with primers TEF-Hyg-P1 and TEF-Hyg-P2 (FIG. 3) (See, Table 1 for primer sequences). The resultant plasmid served as template for PCR amplification of the overlapping split marker regions using primer combinations, a) PKS4-P1 and Hyg-P2; and b) PKS4-P4 and Hyg-P1 (See, Table 1 for primer sequences). The resulting PCR product formed the PKS knockout cassette (SEQ ID NO. 7). The DNA fragments were purified by column separation or ethanol precipitation; and then used in equimolar amounts for transformation of A. pullulans NRRL 50384. Transformation was carried using electroporation as previously described (Varma, et al., Infect. Immun., 60(3):1101-8 (1992)) using logarithmically growing cells. After electroporation, cells were recovered for 3 hr in YPD medium (1% YE, 2% peptone, 2% glucose) prior to plating on YPD-Hyg plates containing 100 μg/ml hygromycin B.

Isolates were transferred at least two times on YPD-Hyg plates and then screened by PCR amplification to confirm the following integration patterns: (1) 5′ cross-over integration of the transforming DNA using PKS4-P5 and Hyg-P10, (2) 3′ cross-over integration of the transforming DNA using PKS4-P6 and Hyg P13, and (3) deletion of the native pks4 gene using primers PKS4-P7 and PKS4-P8 (See, Table 1 for primer sequences). Primers PKS4-P5 and PKS4-P6 both anneal outside of the homologous regions of the transforming DNA so PCR amplification as described is persuasive evidence of gene replacement as designed.

Isolates were transferred at least two times on selective medium and then screened for PCR amplification of the 5′ and 3′ integration junctions; and deletion of the native gene, which would only occur with integration of the constructed DNA fragment. Confirmed deletion isolates were chosen for further analyses. The resulting strain lacking a functional PKS4 gene was termed PksKO.

Example 6

To determine whether a PksKO strain was capable of producing a desired bioproduct (liamocins) without melanin contamination, liamocins were produced and purified as previously described (Manitchotpisit, 2011, ibid.). NRRL 50384 and PksKO strains were utilized for this analysis. Cultures were grown with 50 g/L sucrose, the isolated knock-out (KO) transformant had no melanin-pigment accumulation in the cultures (FIG. 6) and the final product had superior clarity (FIG. 7). There was not any statistical difference in liamocin yield (data not shown) and the molecular structures (FIG. 8) were the same between the parent and KO strains.

Example 7

Deleting multiple genes in A. pullulans is more convenient with the availability of multiple selectable markers, so we created a ura3 auxotroph in A. pullulans. Using the sequenced genome of A. pullulans NRRL 50384, we identified an orotidine 5′phosphate decarboxylase gene that was homologus to another previously described ura3 gene. A Ura3 disruption plasmid was constructed by Gibson assembly using the following PCR fragments: (1) pUC18 amplified with primers pUC18-P1 and pUC18-P1, (2) Ura3 5′ region amplified with primers Ura3-P1Gib and Ura3-P5Gib using A. pullulans NRRL 50384 DNA as template, and (3) Ura3 3′ region amplified with primers Ura3-P4Gib and Ura4-P6Gib using A. pullulans NRRL 50384 DNA as template. The resultant plasmid served as a template for PCR amplification using primers Ura3-P1 and Ura3-P4. The DNA fragment were purified by column separation or ethanol precipitation; and then used for transformation of A. pullulans NRRL 50384. Transformation was carried using electroporation as previously described using logarithmically growing cells. After electroporation, cells were transferred to yeast nitrogen base without amino acids (YNB, Difco) supplemented with 2% glucose and 50 mg/L uracil, and 1 mg/ml 5-fluoroorotic (FOA) acid for selection of uracil auxotrophs. Isolates were transferred at least two times on YNB-FOA plates and then screened on YNB with and without uracil. All of the recovered isolates were confirmed uracil auxotrophs with mutations in the ura3 gene. We further established that at least one of the isolates, A. pullulans B44p41-01, could be restored to uracil prototrophy by transformation with a ura3 DNA fragment obtained from PCR amplification using primers Ura3-P7 and Ura-P8.

Example 8

Using the sequenced genome of A. pullulans NRRL 50384, we identified two MDH genes that are likely involved in conversion between mannitol and fructose. We deleted the first of these genes, termed “MDH1”. A MDH1 disruption plasmid was constructed by Gibson assembly using the following PCR fragments: (1) pUC18 was amplified with primers pUC18-P1 and pUC18-P1, (2) MDH1 5′ region was amplified with primers Mdh1-P1Gib and Mdh1-P2Gib, (3) MDH1 3′ region was amplified with primers Mdh1-P3Gib and Mdh1-P4Gib, and (4) the 2.5 kb ura3 cassette previously amplified with primers Ura3-P7 and Ura3-P8 (See, Table 1 for primer sequences). The resultant plasmid served as template for PCR amplification of the overlapping split marker regions using primer combinations, a) Mdh1-P1 and Ura3-P13; and b) Mdh1-P4 and Ura3-P15 (See, Table 1 for primer sequences). The DNA fragments were purified by column separation or ethanol precipitation; and then used in equimolar amounts for transformation of A. pullulans NRRL 50384. Transformants with confirmed integration and deletion of the mdh1 gene, as indicated by PCR amplification, were then used as a recipient strain for transformation with the overlapping MPD1-Hyg fragments as described above. Resulting knockout strains were analyzed for intracellular polyols, as previously described. The results show that neither A. pullulans (mdh1) nor A. pullulans (mdh1, mpd1) had significant differences in intracellular mannitol, arabitol, glycerol, and trehalose compared with A. pullulans NRRL 50384. However, both mdh1 deletion strains were incapable of growth in YNB (2% mannitol), while A. pullulans NRRL 50384 and A. pullulans (mpd1) were able to achieve OD600>8.0 after 48 hrs.

Example 9

Deletion of the second putative MDH-encoding gene (termed “MDH2”) that was identified can be achieved using the same scheme as outlined above. The resulting strain is termed Mdh2KO. A MDH2 disruption plasmid is constructed by Gibson assembly using the following PCR fragments: (1) pUC18 amplified with primers pUC18-P1 and pUC18-P1, (2) MDH2 5′ region amplified with primers Mdh2-P1Gib and Mdh2-P2Gib, (3) MDH2 3′ region amplified with primers Mdh2-P3Gib and Mdh2-P4Gib, and (4) the 2.5 kb ura3 cassette previously amplified with primers Ura3-P7 and Ura3-P8 (See, Table 1 for primer sequences). The resultant plasmid serves as template for PCR amplification of the overlapping split marker regions using primer combinations, a) Mdh2-P1 and Ura3-P13; and b) Mdh2-P4 and Ura3-P15. The DNA fragments are purified by column separation or ethanol precipitation; and then used in equimolar amounts for transformation of A. pullulans NRRL 50384.

To analyze whether deletion of the MDH2 gene shifted bioproduct production in genetically altered A. pullulans strains, liamocins are produced, purified and analyzed as previously described (Manitchotpisit, 2011, ibid.). Transformant A. pullulans (mdh2) served as a recipient strain for further deletion of mpd1 as described in Example 2. Cultures of A. pullulans (mdh2), A. pullulans (mdh2, mpd1) and A. pullulans NRRL 50384 were grown in the presence of 50 g/L glucose or 50 g/L fructose and differences in intracellular mannitol, arabitol, glycerol, trehalose, and fructose are analyzed as described in Example 3, but are expressed based on cell dry weight in Table 3, where standard deviations are in parentheses and quantities with statistically different values compared with NRRL 50384 controls grown under the same conditions are marked with asterisks (p<0.05 with T-Test).

TABLE 3 Polyol and fructose accumulation in WT, Mdh2KO, and Mdh2.Mpd1KO strains Intracellular concentrations (μg/mg cell dry weight) Strain/carbon source Mannitol Arabitol Glycerol Trehalose Fructose 50384/glucose 67.1 (5.3) 5.0 (0.9) 2.7 (0.1) 125.7 (6.5)  0 Mdh2KO/glucose 66.9 (3.9) 3.8 (0.1) 2.7 (0.1) 117.0 (2.5)  0 Mdh2KO/Mpd1KO/glucose 0* 3.0 (0.4)  5.8 (0.2)* 181.7 (8.8)* 0 50384/fructose 147.8 (8.4)  0.7 (1.0) 2.0 (0.6) 17.2 (0.8)  80.8 (26.3) Mdh2KO/fructose 102.2 (3.5)* 0.5 (0.0) 3.3 (0.1)  54.6 (2.7)* 37.9 (3.2) Mdh2KO/Mpd1KO/fructose  6.1 (0.2)*  1.7 (0.1)*  6.8 (0.1)*  99.6 (1.8)* 61.0 (1.5)

There was not any significant decrease in mannitol for the Mdh2KO strain compared with the parent isolate when grown on glucose. However, the Mdh2KO/Mpd1KO strain did not have any detectable mannitol under these same conditions. Arabitol was only slightly less for the two modified strains, but the Mdh2KO/Mpd1KO strain had more than 2-fold increase in glycerol and nearly 50% increase in trehalose compared with the parent strain. The Mdh2KO strain did not show any difference in the levels of these compounds compared with the parent strain under these conditions.

When grown on fructose, there was a slight decrease in the mannitol for the Mdh2KO strain compared with the parent isolate, while the Mdh2KO/Mpd1KO strain had more than 95% less mannitol compared with the control. Under these same conditions, the Mdh2KO/Mpd1KO strain also had significantly higher concentrations of arabitol, glycerol, and trehalose compared with the parent strain. The Mdh2KO strain had significantly higher trehalose compared with the control.

Further analysis of these cultures revealed that the Mdh2KO strain produced nearly 100% mannitol-containing liamocin (FIGS. 10 and 11) with both glucose and fructose in a similar manner as the parent strain (FIGS. 4 and 5). The Mdh2KO/Mpd1KO strain produced significant amounts of arabitol-containing liamocin with glucose (FIG. 10), but exophilins (i.e., liamocin without a polyol or carbohydrate headgroup) appeared to be the predominant structure under these conditions. The Mdh2KO/Mpd1KO strain grown with fructose also appeared to have a predominance of exophilins, but also contained significant amounts of a surprisingly unique structure containing fructose as a headgroup (FIG. 11). The assignment of the fructose head group was further confirmed by hydrolyzing liamocin samples using 2M TFA (80° C., 1 hr), partitioning with aqueous chloroform to remove the released fatty acids, and peracetylating the released fructose in the aqueous layer (using acetic anhydride, pyridine 1:1 v/v, 80° C., 30 min). The peracetylated headgroup components were analyzed by gas chromatography (FIG. 12), and the structural assignment of the peracetylated fructose was confirmed by GC/MS. The structure of these fructose-type liamocins has not been previously described and has never been observed to be formed by WT strains.

Example 10

As another example, we report on the simplified purification of massoia lactone from A. pullulans strain PksKO. In analyzing the PksKO strain, we discovered that this strain produced massoia lactone, a bioproduct never before identified as produced by A. pullulans. However, selective extraction of the cultures of the Aureobasidium PksKO strain with butan-2-one followed by butan-2-one:chloroform:water (1:2:2 by volume) partitioning recovered a product identical to massoia lactone (1H-NMR, 13C-NMR, COSY, HSQC, HMBC, and MALDI-TOF MS analyses. 13C-NMR chemical shifts (in CDCl3): C1 C═O, 165.46 ppm; C2 CH, 121.26 ppm; C3 CH, 145.61 ppm; C4 CH2, 29.36 ppm; C5 CH 78.31 ppm; C6 CH2, 34.76 ppm; C7 CH2, 24.45 ppm; C8 CH2, 31.50 ppm; C9 CH2, 22.47 ppm; C10 CH3, 13.94 ppm. M=m/z 168; [M=Na]+=m/z 191. The massoia lactone was of high purity (FIG. 9), and the NMR data was obtained without the need for chromatography clean-up. Determination of yield can be determined gravimetrically using A. pullulans PksKO. Purification of liamocins will be as previously described, followed by butan-2-one:chloroform:water (1:2:2 by volume) partitioning to recover massoia lactone. 

What is claimed is:
 1. A method of producing arabitol-liamocins, comprising the steps of a) growing a culture of Aureobasidium pullulans lacking a functional mannitol-1-phosphate-dehydrogenase (MPD1) gene under conditions sufficient to support the production of arabitol-liamocins, wherein said conditions comprise a medium that is substantially free of arabitol; and b) collecting said arabitol-liamocins from at least part of said culture, thereby producing arabitol-liamocins.
 2. The method of claim 1, wherein the Aureobasidium pullulans strain comprises NRRL
 67079. 3. The method of claim 1, wherein said conditions further comprise a growth medium containing glucose as the sole carbon source.
 4. A method of producing one or more bioproducts, comprising the steps of a) growing a culture of Aureobasidium pullulans lacking a functional mannitol-dehydrogenase (MDH2) gene and lacking a functional mannitol-1-phosphate-dehydrogenase (MPD1) gene under conditions sufficient to support the production of one or more bioproducts selected from the group consisting of a liamocin and an exophilin; and b) collecting said one or more bioproducts from at least part of said culture, thereby producing the bioproduct.
 5. The method of claim 4, wherein said conditions comprise a growth medium containing glucose or fructose as the sole carbon source.
 6. The method of claim 4, wherein the bioproduct is an exophilin.
 7. The method of claim 4, wherein the bioproduct is a liamocin and wherein said liamocin has a head group comprising lactose, glucose, mannose, galactose, arabinose, xylose, glucitol, galactitol, xylitol, ribitol, threitol, erythritol, or glycerol.
 8. The method of claim 4, wherein the bioproduct is a fructose-liamocin. 